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Gymnastics and Multicomponent Training Intervention in Community-dwelling Older Adults

11 de agosto de 2026 actualizado por: Marcos Luciano Pimenta Pinheiro, Federal University of the Valleys of Jequitinhonha and Mucuri

Community-based Multicomponent Training and Gymnastics Intervention

Introduction: Extension projects focused on physical activity can offer health practices and promote quality of life for participants of different ages. Investing in extension projects with a research interface can contribute to relevant insights for teaching knowledge. Furthermore, the progressive aging of the population makes it essential to identify individuals at risk of functional decline and to implement evidence-based interventions that allow for the reduction of these losses, enabling a better quality of life for the elderly. The WHO developed the guideline that addresses healthy development, with strategies to promote healthy aging based on solid concepts, with data on their applicability in a real-life scenario, especially from intervention studies. Objective: To evaluate the impact of interventions focused on Gymnastics and multicomponent training on the intrinsic capacity of adult and elderly participants in extension projects at UFBA. Methodology: This is an intervention study within an extension project with a research focus, encompassing adult individuals (participants in MOVEGINBA) and elderly individuals of both sexes, aged 60 years or older (participants in the MOVEGINBA 60+ project). Participants will be evaluated regarding anthropometric, sociodemographic characteristics, health conditions, and physical-functional performance. As well as quality of life, sleep quality, fear of falling, and independence in activities of daily living. Tests and interviews will be conducted before and after the intervention. The results of this study will be fundamental to understanding the implications of the multicomponent gymnastics/training intervention for the participants.

Keywords: Aging; Physical capacity; Gymnastics.

Descripción general del estudio

Descripción detallada

University outreach programs should be offered to promote the health and quality of life of the general population, taking into account diverse target audiences. Viewing outreach as an extension of the university into the community, the MOVEGINBA project-registered with PROEXC under number 23132-has been conducted in the Faculty of Education's exercise studio since the first semester of 2025, serving adults, students from various academic programs, and the general public through training activities. Concurrently, the global population is aging rapidly, with significant impacts on economies and healthcare systems. In Brazil, the population aged 65 and older is projected to rise from the current 20 million in 2020 (9.8% of the population) to over 50 million by 2050 (21.8% of the population). Given this scenario, public policies capable of mitigating age-related loss of functional capacity are both urgent and essential. In its report on health and aging, the WHO defined healthy aging as a process requiring the promotion and maintenance of functional capacities that enable individual well-being. Thus, optimizing the health of older adults through strategies that identify high-risk individuals and propose actions to prevent or delay the progression of functional decline appears to be the best approach to reducing the strain on healthcare systems.

In 2017, the WHO published guidelines for healthy development, which address health and well-being and encompass physical activity for individuals. With this perspective in mind, extension activities are encouraged and take place within the university setting, focusing on older adults; to this end, we offer the MOVEGINBA 60+ program-registered with PROEXC under number 23351-which addresses the specific gaps and needs of this demographic. Consequently, gymnastics-based extension projects are conducted at the Federal University of Bahia.

It is essential to understand the implications of such projects for participants regarding emotional health, physical capacity, agility, social interaction, and the intrinsic capacity of older adults. Therefore, this study aims to understand the implications of gymnastics-focused interventions for participants and to analyze their impact on the target population. This initiative is an extension project with a research component-encompassing undergraduate capstone projects and graduate studies-that contributes significantly to people's quality of life.

Conditions: Must be an older adult (over 60 years of age). Must be capable of performing any physical activity independently. Participants may have hypertension, diabetes, or multiple comorbidities, provided they fall within the 1 to 7 range on the Clinical Frailty Scale (ranging from robust to mildly frail).

Tipo de estudio

Intervencionista

Inscripción (Estimado)

80

Fase

  • Fase 1

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

    • Estado de Bahia
      • Salvador, Estado de Bahia, Brasil, 40170115
        • Faculdade de Educação

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

Sí

Descripción

Inclusion criteria: Community-dwelling older adults (60 years of age or older), and able to travel to the training center.

Exclusion criteria: Score 7, 8 or 9 on the Clinical Frailty Scale and those with any impediment to performing physical exercise.

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Prevención
  • Asignación: N / A
  • Modelo Intervencionista: Asignación de un solo grupo
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Multicomponent training intervention
Multicomponent training intervention - Protocol includes mobility, resistance exercises for the lower and upper limbs and major muscle groups, and aerobic exercises. The intervention will take place twice a week for one hour, following a 12-week protocol.

The interventions will take place twice a week, on two days (Mondays and Wednesdays) with two groups lasting one hour each. The exercises will include joint mobility training, followed by strength training with body weight and the use of elastic bands, dumbbells, sticks, and the like. Subsequently, there will be an aerobic part, lasting 30 minutes, in which the heart rate will be increased, with the use of sound and rhythms. Following this, there will be a cool-down, with a reduction in activities.

Participants will be evaluated before and after the intervention, after 12 weeks, with variables that include intrinsic capacity such as mobility, psychological state, vitality, sensory and cognitive domain.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Intrinsic capacity
Periodo de tiempo: Sample collected before the intervention. Subsequently, another sample was collected 12 weeks after the intervention.
Cognition: Montreal Cognitive Assessment - MOCA
Sample collected before the intervention. Subsequently, another sample was collected 12 weeks after the intervention.
Intrinsic capacity
Periodo de tiempo: Sample collected before the intervention. Subsequently, another sample was collected 12 weeks after the intervention.
Mobility: 5-times sit-to-stand test and 6-minutr walk test
Sample collected before the intervention. Subsequently, another sample was collected 12 weeks after the intervention.
Intrinsic capacity
Periodo de tiempo: Sample collected before the intervention. Subsequently, another sample was collected 12 weeks after the intervention.
Psychological:15 itens - Geriatric Depression Scale -GDS-15
Sample collected before the intervention. Subsequently, another sample was collected 12 weeks after the intervention.
Intrinsic capacity
Periodo de tiempo: Sample collected before the intervention. Subsequently, another sample was collected 12 weeks after the intervention.
Vitality: Handgrip strength
Sample collected before the intervention. Subsequently, another sample was collected 12 weeks after the intervention.
Intrinsic capacity:
Periodo de tiempo: Sample collected before the intervention. Subsequently, another sample was collected 12 weeks after the intervention.
Hearing: Self-reported - Self-reported - Participants are asked if they have any hearing problems.
Sample collected before the intervention. Subsequently, another sample was collected 12 weeks after the intervention.
Intrinsic capacity
Periodo de tiempo: Sample collected before the intervention. Subsequently, another sample was collected 12 weeks after the intervention.
Vision: self-reported - Participants are asked if they have any vision problems, if they have difficulty seeing up close or far away, if they have any eye disease, or if they are undergoing medical treatment for diabetes or hypertension.
Sample collected before the intervention. Subsequently, another sample was collected 12 weeks after the intervention.

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Anthropometry
Periodo de tiempo: Sample collected before the intervention. Subsequently, another sample was collected 12 weeks after the intervention.
BMI: Weight and height will be used to calculate Body Mass Index.
Sample collected before the intervention. Subsequently, another sample was collected 12 weeks after the intervention.

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Publicaciones y enlaces útiles

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Enlaces Útiles

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

20 de febrero de 2026

Finalización primaria (Estimado)

20 de diciembre de 2027

Finalización del estudio (Estimado)

20 de diciembre de 2028

Fechas de registro del estudio

Enviado por primera vez

26 de mayo de 2026

Primero enviado que cumplió con los criterios de control de calidad

11 de agosto de 2026

Publicado por primera vez (Actual)

17 de agosto de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

17 de agosto de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

11 de agosto de 2026

Última verificación

1 de agosto de 2026

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Descripción del plan IPD

Due to participant confidentiality, the data may be shared, but participant identification will not be disclosed.

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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